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Eriocalyxin B ameliorates experimental autoimmune encephalomyelitis by suppressing Th1 and Th17 cells

Proceedings of the National Academy of Sciences - PNAS, 2013-02, Vol.110 (6), p.2258-2263

2013

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PALLD Regulates Phagocytosis by Enabling Timely Actin Polymerization and Depolymerization

The Journal of immunology (1950), 2017-09, Vol.199 (5), p.1817-1826

2017

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Preferential eradication of acute myelogenous leukemia stem cells by fenretinide

Proceedings of the National Academy of Sciences - PNAS, 2013-04, Vol.110 (14), p.5606-5611

2013

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Structural framework of c-Src activation by integrin β3

Blood, 2013-01, Vol.121 (4), p.700-706

2013

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Role and Mechanism of the Interaction of BCR-ABL with E3 Ligase c-CBL in Targeting Therapy of Chronic Myelogenous Leukemia

Zhongguo shi yan xue ye xue za zhi, 2017-02, Vol.25 (1), p.42

2017

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Homoharringtonine deregulates MYC transcriptional expression by directly binding NF-κB repressing factor

Proceedings of the National Academy of Sciences - PNAS, 2019-02, Vol.116 (6), p.2220-2225

2019

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Gene therapy for hemophilia B

Zhōnghuá xuèyèxué zázhì, 2013-09, Vol.34 (9), p.809-811

2013

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An atom-efficient and powerful method for direct esterification of silyl ethers catalyzed by HClO4―SiO2

Tetrahedron, 2011-02, Vol.67 (6), p.1096-1101

2011

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Effect of the Integrin β3 Cytoplasmic NITY Motif on α II bβ3-Mediated Cell Functions in CHO Cell Model

Zhongguo shi yan xue ye xue za zhi, 2015-06, Vol.23 (3), p.768

2015

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Myr-RKEFAK Peptide Selectively Regulates Outside-in Signaling Transduction-related Functions in Human Platelets

Zhongguo shi yan xue ye xue za zhi, 2015-06, Vol.23 (3), p.761

2015

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Inherent hepatocytic heterogeneity determines expression and retention of edited F9 alleles post-AAV/CRISPR infusion

Proceedings of the National Academy of Sciences - PNAS, 2021-10, Vol.118 (42), p.1

2021

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Trans-repressive effect of NUP98-PMX1 on PMX1-regulated c-fos gene through recruitment of histone deacetylase 1 by FG repeats

Cancer research (Chicago, Ill.), 2006-05, Vol.66 (9), p.4584-4590

2006

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Research progress on the effect of shear stress on thrombosis

Zhōnghuá xīnxuèguănbìng zázhì, 2013-10, Vol.41 (10), p.893

2013

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The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

Zhōnghuá xuèyèxué zázhì, 2013-08, Vol.34 (8), p.691-695

2013

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A single E726Q mutation in the membrane proximal α-helix of integrin β3 subunit induces membrane blebbing by disrupting the membrane-actin cortex interaction

Zhongguo shi yan xue ye xue za zhi, 2011-12, Vol.19 (6), p.1450

2011

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RIG-I Modulates Src-Mediated AKT Activation to Restrain Leukemic Stemness

Molecular cell, 2014-02, Vol.53 (3), p.407-419

2014

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Transgenic mouse models of the truncated platelet integrin β3 cytoplasmic tail established by stem cell transplantation

Zhongguo shi yan xue ye xue za zhi, 2013-06, Vol.21 (3), p.667

2013

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Long-Term Outcome of Photobiomodulation Therapy for Refractory Diabetic Wound After Secretory Carcinoma of the Parotid Gland Surgery: A Case Report

Photobiomodulation, photomedicine, and laser surgery, 2024-05, Vol.42 (5), p.383

2024

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Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain

Zhōnghuá xuèyèxué zázhì, 2013-03, Vol.34 (3), p.190-194

2013

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Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases

Zhonghua yi xue yi chuan xue za zhi, 2012-10, Vol.29 (5), p.524

2012

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The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease

Chung-hua nei kʿo tsa chih, 2012-10, Vol.51 (10), p.788

2012

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Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation

Zhōnghuá xuèyèxué zázhì, 2011-09, Vol.32 (9), p.587-591

2011

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A Novel Air-Cooled Nd:YAG Laser for the Treatment of the Venous Lakes of the Lips

Photobiomodulation, photomedicine, and laser surgery, 2024-03, Vol.42 (3), p.230

2024

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Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain

Zhōnghuá xuèyèxué zázhì, 2012-06, Vol.33 (6), p.475-479

2012

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Two novel mutations in one pedigree with hereditary Factor VII deficiency

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.158-162

2011

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Eriocalyxin B ameliorates experimental autoimmune encephalomyelitis by suppressing Th1 and Th17 cells

PALLD Regulates Phagocytosis by Enabling Timely Actin Polymerization and Depolymerization

Preferential eradication of acute myelogenous leukemia stem cells by fenretinide

Structural framework of c-Src activation by integrin β3

Role and Mechanism of the Interaction of BCR-ABL with E3 Ligase c-CBL in Targeting Therapy of Chronic Myelogenous Leukemia

Homoharringtonine deregulates MYC transcriptional expression by directly binding NF-κB repressing factor

Gene therapy for hemophilia B

An atom-efficient and powerful method for direct esterification of silyl ethers catalyzed by HClO4―SiO2

Effect of the Integrin β3 Cytoplasmic NITY Motif on α II bβ3-Mediated Cell Functions in CHO Cell Model

Myr-RKEFAK Peptide Selectively Regulates Outside-in Signaling Transduction-related Functions in Human Platelets

Inherent hepatocytic heterogeneity determines expression and retention of edited F9 alleles post-AAV/CRISPR infusion

Trans-repressive effect of NUP98-PMX1 on PMX1-regulated c-fos gene through recruitment of histone deacetylase 1 by FG repeats

Research progress on the effect of shear stress on thrombosis

The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

A single E726Q mutation in the membrane proximal α-helix of integrin β3 subunit induces membrane blebbing by disrupting the membrane-actin cortex interaction

RIG-I Modulates Src-Mediated AKT Activation to Restrain Leukemic Stemness

Transgenic mouse models of the truncated platelet integrin β3 cytoplasmic tail established by stem cell transplantation

Long-Term Outcome of Photobiomodulation Therapy for Refractory Diabetic Wound After Secretory Carcinoma of the Parotid Gland Surgery: A Case Report

Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain

Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases

The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease

Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation

A Novel Air-Cooled Nd:YAG Laser for the Treatment of the Venous Lakes of the Lips

Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain

Two novel mutations in one pedigree with hereditary Factor VII deficiency

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